| Identification | More | [Name]
PHYTOL | [CAS]
150-86-7 | [Synonyms]
3,7,11,15-TETRAMETHYL-2-HEXADECEN-1-OL
PHYTOL
[R*,R*-(E)]-3,7,11,15-TETRAMETHYL-2-HEXADECEN-1-OL
(E)-3,7,11,15-Tetramethyl-2-hexadedcen-1-ol
(E)-phytol
2,6,10,14-Tetramethylhexadec-14-en-16-ol
2-Hexadecen-1-ol, 3,7,11,15-tetramethyl-, [R-[R*,R*-(E)]]-
3,7,11,15-tetramethyl-,(r-(r*,r*-(e)))-2-hexadecen-1-o
3,7,11,15-tetramethyl-,[R-(R*,R*-(E))]-2-Hexadedcen-1-ol
3,7,11,15-tetramethyl-,[theta-[theta,theta-(e)]]-2-hexadecen-1-o
Plantalcohol
trans-Phytol
phytol, mixture of isomers
3,7,11,15-tetramethylhexadec-2-en-1-ol
Phytolsynthetic
2-Hexadecen-1-ol, 3,7,11,15-tetramethyl-, (2E,7R,11R)-
(E,7R,11R)-3,7,11,15-tetramethylhexadec-2-en-1-ol
(2E,7R,11R)-3,7,11,15-Tetramethyl-2-hexadecen-1-ol
(7R,11R,2E)-3,7,11,15-Tetramethyl-2-hexadecen-1-ol
(7R,11R,E)-3,7,11,15-Tetramethyl-2-hexadecene-1-ol | [EINECS(EC#)]
205-776-6 | [Molecular Formula]
C20H40O | [MDL Number]
MFCD00151280 | [Molecular Weight]
296.53 | [MOL File]
150-86-7.mol |
| Chemical Properties | Back Directory | [Melting point ]
<25 °C | [Boiling point ]
202-204 °C (10 mmHg)
| [density ]
0.85
| [FEMA ]
4196 | PHYTOL | [refractive index ]
1.461-1.469
| [Fp ]
179℃ (Cleveland open test) | [storage temp. ]
Inert atmosphere,2-8°C | [solubility ]
Chloroform, Methanol (Sparingly) | [form ]
Oil | [pka]
14.45±0.10(Predicted) | [color ]
Light Yellow to Yellow | [Odor]
at 100.00 %. delicate floral balsam powdery waxy | [Odor Type]
floral | [JECFA Number]
1832 | [Merck ]
7390 | [Henry's Law Constant]
1.0×10-2 mol/(m3Pa) at 25℃, Ebert et al. (2023) | [Stability:]
Light Sensitive | [Cosmetics Ingredients Functions]
SKIN CONDITIONING - EMOLLIENT
PERFUMING
FRAGRANCE | [InChIKey]
BOTWFXYSPFMFNR-PFIWFTBQSA-N | [LogP]
8.23 | [CAS DataBase Reference]
150-86-7(CAS DataBase Reference) | [EPA Substance Registry System]
Phytol (150-86-7) |
| Safety Data | Back Directory | [Symbol(GHS) ]
   
GHS05,GHS07,GHS08,GHS09 | [Signal word ]
Danger | [Hazard statements ]
H302-H318-H360-H370-H372-H317-H411 | [Precautionary statements ]
P501-P273-P272-P260-P270-P202-P201-P264-P280-P302+P352-P391-P308+P311-P362+P364-P333+P313-P301+P312+P330-P305+P351+P338+P310-P405 | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S37/39:Wear suitable gloves and eye/face protection .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . | [RTECS ]
TJ3490000 | [TSCA ]
TSCA listed | [REACH Registrations]
Active | [HS Code ]
29052290 | [Safety Profile]
Low toxicity by
ingestion and skin contact. A skin irritant.
When heated to decomposition it emits
acrid smoke and irritating fumes. | [Toxicity]
rabbit,LD50,skin,> 5gm/kg (5000mg/kg),Food and Chemical Toxicology. Vol. 20, Pg. 811, 1982. |
| Hazard Information | Back Directory | [Description]
Phytol is a diterpene alcohol obtained from the degradation of chlorophyll and has been used in the synthesis of Vitamins E and K. During the digestion process of ruminants, phytol is liberated from chlorophyll and converted to phytanic acid (Item No. 90360) to be stored in fats. While humans cannot derive phytol from chlorophyll, free phytol, obtained from the consumption of ruminant adipose tissue and dairy products, is readily absorbed in the small intestine and converted to phytanic acid.1 Phytanic acid accumulates to toxic levels in a number of metabolic disorders, and the conversion of phytol to phytanic acid has been shown to be regulated via the activation of peroxisome proliferator-activated receptor α (PPARα).2,1 Phytol and its metabolites have also been reported to activate retinoid X receptors (RXRs; Kis range from 2.3-67.2 μM) and to promote the activity of PPAR/RXR heterodimers.3,2 Phytol also demonstrates sedative and anxiolytic effects through interaction with the GABAA receptor, and it has been explored as an antischistosomal agent in a mouse model of schistosomiasis.4,5 | [Chemical Properties]
Colorless to yellow liquid | [Chemical Properties]
Colorless to yellow viscous liquid; faint floral aroma. | [Occurrence]
Reported found in Herniaria incana lam oil Greece (2.60%) and Witch hazel leaf oil (9.79%). | [Uses]
Preparation of vitamins E and K1. | [Definition]
ChEBI: A diterpenoid that is hexadec-2-en-1-ol substituted by methyl groups at positions 3, 7, 11 and 15. | [Production Methods]
Phytol can be obtained from natural raw materials by a variety of processes. The industrial synthesis of phytol starts from isophytol. The latter is first treated with formic acid to give phytyl formate, from which (Z, E )-phytol (isomer ratio 3 : 7) is obtained by saponification or transesterification. | [Aroma threshold values]
Low strength odor, floral type. |
|
| Company Name: |
J & K SCIENTIFIC LTD.
|
| Telephone: |
18210857532 18210857532 |
| Website: |
https://www.jkchemical.com |
| Company Name: |
Energy Chemical
|
| Telephone: |
400-0056266 |
| Website: |
www.energy-chemical.com |
|